CLASS II Food recall · Reported 25 Dec 2013 · FDA Enforcement Report

Source Naturals Essential Enzyme Ultra Vegi-cap recalled

Threshold Enterprises is recalling Source Naturals Essential Enzyme Ultra Vegi-cap: Premium Digestive Enzyme Blend, distributed nationwide in the US. The recall was initiated on 22 Nov 2013 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesSN2329 Veg Cap 30 ct: Lot numbers FG-38147, FG-41401, Exp 4/20/2017; Lot numbers FG-31309, FG-35193 and FG-37071, Exp. 8/20/2016; UPC# 021078023296) Lot number FG-26565, Exp. 8/20/14. SN2330 Veg Cap 60 ct; Lot numbers FG-37072, FG-41218, Exp 4/20/2017; Lot numbers FG-26566, FG-31091, Exp 8/20/2016; Lot number FG-26566, Exp. 8/20/2014. SN2331 Veg Cap 90 ct; Lot number FG-37073, Exp 4/20/2017; Lot numbers FG-33524, FG-35564, Exp 8/20/2016; Lot number FG-26567, Exp 8/20/2014; SN2332 Veg Cap 120 ct: Lot numbers FG-37462, FG-40028, FG-41219, Exp. 4/20/2017; Lot numbers FG-34174, FG-35723, FG-36310, FG-39575, Exp 8/20/2016; Lot numbers FG-26568, FG-29388, Exp. 8/20/2014 SN7342 Veg Cap 30 + 30 ct. Lot number FG-37074, Exp. 8/20/2016.

Quantity recalled12,352 bottles, all counts

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number: F-1100-2014
FDA event ID: 66954
Recalling firm: Threshold Enterprises, Scotts Valley, CA
Brand: Source Naturals
Classification: Class II
Status: Terminated
Recall initiated: 22 Nov 2013
FDA classified: 17 Dec 2013
Reported: 25 Dec 2013
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Other Reasons
Product category: Probiotics

Timeline

22 Nov 2013	Recall initiated by company
17 Dec 2013	Classified by FDA	+25 days
25 Dec 2013	Published in enforcement report	+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Dietary Supplements were made with bulk products provided by National Enzyme Company which are currently under recall for chloramphenicol

Product as listed by the FDA

Source Naturals Essential Enzyme Ultra VEGI-CAP: Premium Digestive Enzyme Blend; 30, 60, 90 & 120 count bottles. Vegetarian capsules Manufactured for: Source Naturals, Inc. Santa Cruz, CA

Where it was distributed

Nationwide distribution

Nationwide

Questions about this recall

Is Source Naturals Essential Enzyme Ultra Vegi-cap: Premium Digestive Enzyme Blend recalled?

Yes. Threshold Enterprises recalled Source Naturals Essential Enzyme Ultra Vegi-cap: Premium Digestive Enzyme Blend on 22 Nov 2013. The recall is Class II and its status is Terminated. Recall number F-1100-2014.

Why was it recalled?

Dietary Supplements were made with bulk products provided by National Enzyme Company which are currently under recall for chloramphenicol

Which lots are affected?

SN2329 Veg Cap 30 ct: Lot numbers FG-38147, FG-41401, Exp 4/20/2017; Lot numbers FG-31309, FG-35193 and FG-37071, Exp. 8/20/2016; UPC# 021078023296) Lot number FG-26565, Exp. 8/20/14. SN2330 Veg Cap 60 ct; Lot numbers FG-37072, FG-41218, Exp 4/20/2017; Lot numbers FG-26566, FG-31091, Exp 8/20/2016; Lot number FG-26566, Exp. 8/20/2014. SN2331 Veg Cap 90 ct; Lot number FG-37073, Exp 4/20/2017; Lot numbers FG-33524, FG-35564, Exp 8/20/2016; Lot number FG-26567, Exp 8/20/2014; SN2332 Veg Cap 120 ct: Lot numbers FG-37462, FG-40028, FG-41219, Exp. 4/20/2017; Lot numbers FG-34174, FG-35723, FG-36310, FG-39575, Exp 8/20/2016; Lot numbers FG-26568, FG-29388, Exp. 8/20/2014 SN7342 Veg Cap 30 + 30 ct. Lot number FG-37074, Exp. 8/20/2016.

Where was it sold?

Nationwide distribution

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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